about
One hundred years of vitamins-a success story of the natural sciences.Copper-Catalyzed Transformations Using Cu-H, Cu-B, and Cu-Si as Active Catalyst Species.5',6'-nucleoside phosphonate analogues architecture: synthesis and comparative evaluation towards metabolic enzymes.Chemistry and biochemistry of unsaturated fatty acids.Increasing the structural span of alkyne metathesis.Selective semihydrogenation of alkynes on shape-controlled palladium nanocrystals.Iron pincer complex catalyzed, environmentally benign, E-selective semi-hydrogenation of alkynes.Palladium catalysed alkyne hydrogenation and oligomerisation: a parahydrogen based NMR investigation.MOF-Derived Cobalt Phosphide/Carbon Nanocubes for Selective Hydrogenation of Nitroarenes to Anilines.Stereoselective Transfer Semi-Hydrogenation of Alkynes to E-Olefins with N-Heterocyclic Silylene-Manganese Catalysts.An alkene-promoted borane-catalyzed highly stereoselective hydrogenation of alkynes to give Z- and E-alkenes.Aminoquinoline-assisted vinylic C-H arylation of unsubstituted acrylamide for the selective synthesis of Z olefins.A Pd-Cu2O nanocomposite as an effective synergistic catalyst for selective semi-hydrogenation of the terminal alkynes only.Combining visible light catalysis and transfer hydrogenation for in situ efficient and selective semihydrogenation of alkynes under ambient conditions.Deconvoluting the memory effect in Pd-catalyzed allylic alkylation: Effect of leaving group and added chloride.Einhundert Jahre Vitamine - eine naturwissenschaftliche ErfolgsgeschichteChemie und Biochemie ungesättigter FettsäurenCatalytic Stereoselective Semihydrogenation of Alkynes toE-AlkenesPalladium nanoparticles supported on mpg-C3N4 as active catalyst for semihydrogenation of phenylacetylene under mild conditions
P2860
Q38064805-DDC98A20-6BCC-4BCE-BD03-90638A42D44BQ38887365-65E52E0E-B7FA-4211-BDE5-C56FAB9A5BDBQ39543558-576D919E-96A7-4E9E-9175-EC93BB03783AQ40742636-F1462746-48B6-480F-9A37-AD66AD1C920DQ44157152-5408BA92-3B47-4763-8D63-831432857AE0Q44385959-910077E9-6318-4E69-9487-3502C030E056Q46244478-4CEFB5A7-D6DA-4A53-B3B3-6B65FF048ADFQ46443948-F4B079E9-840C-419B-BA67-8F2C5DA346B2Q47229405-FCF7AB4B-FEC4-422C-B3E4-133C59C53AA6Q48140672-1161821E-2F16-4021-9D5C-D104E64C8AA1Q51017747-E6BB1400-0793-4A85-AAC1-1CE035084C74Q51476137-CE18C1ED-E5B5-47BB-AEBD-CA1AB33D33CDQ51532846-38163D65-346B-4BD9-AF92-FF6CB7063EA3Q51634737-1B2BAB1D-7435-461A-938E-E53DFCD2953BQ51983011-B1A9B926-6D0C-4E1B-820C-820D530CCECBQ56624692-EB9E7017-E6B5-4C35-9F9C-47E09F8BBCBDQ56625604-4A9EDCB6-B023-425A-B043-9F9D52E0455CQ56690363-70D679DC-9C45-45F6-9DB1-E43652A0FB5AQ57586818-B76CDC7D-1C63-4911-8BCB-2BC381900A5C
P2860
description
wetenschappelijk artikel
@nl
наукова стаття, опублікована в 1966
@uk
name
PALLADIUM CATALYST FOR PARTIAL REDUCTION OF ACETYLENES
@en
PALLADIUM CATALYST FOR PARTIAL REDUCTION OF ACETYLENES
@nl
type
label
PALLADIUM CATALYST FOR PARTIAL REDUCTION OF ACETYLENES
@en
PALLADIUM CATALYST FOR PARTIAL REDUCTION OF ACETYLENES
@nl
prefLabel
PALLADIUM CATALYST FOR PARTIAL REDUCTION OF ACETYLENES
@en
PALLADIUM CATALYST FOR PARTIAL REDUCTION OF ACETYLENES
@nl
P356
P1433
P1476
PALLADIUM CATALYST FOR PARTIAL REDUCTION OF ACETYLENES
@en
P356
10.15227/ORGSYN.046.0089
P577
1966-01-01T00:00:00Z